Literature DB >> 10378395

Congenital hydrocephalus internus and aqueduct stenosis: aetiology and implications for genetic counselling.

F Haverkamp1, J Wölfle, M Aretz, A Krämer, B Höhmann, H Fahnenstich, K Zerres.   

Abstract

UNLABELLED: Genetic counselling in families with congenital hydrocephalus internus (CHI) in combination with aqueduct stenosis (AS) is often difficult due to an uncertain aetiology. We present a series of 35 patients with CHI and AS focusing on the aetiology and presumed recurrence risk for siblings. In 13 patients (37.1%) a genetic aetiology was identified with an increased recurrence risk for siblings. The relative frequency of patients with X-linked hydrocephalus in our sample was in accordance with the literature (2/35), but was more frequent in other diseases with Mendelian inheritance.
CONCLUSION: In addition to the well-known X-linked and autosomal recessive forms of aqueduct stenosis with hydrocephalus, this malformation can occur in other diseases with Mendelian inheritance. This finding is of considerable importance for genetic counselling and prognosis.

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Year:  1999        PMID: 10378395     DOI: 10.1007/s004310051123

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  13 in total

1.  A mutation in Ccdc39 causes neonatal hydrocephalus with abnormal motile cilia development in mice.

Authors:  Zakia Abdelhamed; Shawn M Vuong; Lauren Hill; Crystal Shula; Andrew Timms; David Beier; Kenneth Campbell; Francesco T Mangano; Rolf W Stottmann; June Goto
Journal:  Development       Date:  2018-01-09       Impact factor: 6.868

2.  Disruption of the mouse Jhy gene causes abnormal ciliary microtubule patterning and juvenile hydrocephalus.

Authors:  Oliver K Appelbe; Bryan Bollman; Ali Attarwala; Lindy A Triebes; Hilmarie Muniz-Talavera; Daniel J Curry; Jennifer V Schmidt
Journal:  Dev Biol       Date:  2013-07-29       Impact factor: 3.582

3.  De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus.

Authors:  Charuta Gavankar Furey; Jungmin Choi; Sheng Chih Jin; Xue Zeng; Andrew T Timberlake; Carol Nelson-Williams; M Shahid Mansuri; Qiongshi Lu; Daniel Duran; Shreyas Panchagnula; August Allocco; Jason K Karimy; Arjun Khanna; Jonathan R Gaillard; Tyrone DeSpenza; Prince Antwi; Erin Loring; William E Butler; Edward R Smith; Benjamin C Warf; Jennifer M Strahle; David D Limbrick; Phillip B Storm; Gregory Heuer; Eric M Jackson; Bermans J Iskandar; James M Johnston; Irina Tikhonova; Christopher Castaldi; Francesc López-Giráldez; Robert D Bjornson; James R Knight; Kaya Bilguvar; Shrikant Mane; Seth L Alper; Shozeb Haider; Bulent Guclu; Yasar Bayri; Yener Sahin; Michael L J Apuzzo; Charles C Duncan; Michael L DiLuna; Murat Günel; Richard P Lifton; Kristopher T Kahle
Journal:  Neuron       Date:  2018-07-05       Impact factor: 17.173

4.  Dscam mutation leads to hydrocephalus and decreased motor function.

Authors:  Yiliang Xu; Haihong Ye; Yan Shen; Qi Xu; Li Zhu; Jianghong Liu; Jane Y Wu
Journal:  Protein Cell       Date:  2011-09-09       Impact factor: 14.870

5.  A case of congenital syndromic hydrocephalus: a subtype of 'game-friedman-paradice syndrome'.

Authors:  Tapan Kumar Jana; Hironmoy Roy; Susmita Giri
Journal:  Oman Med J       Date:  2013-01

6.  Congenital hydrocephalus associated with abnormal subcommissural organ in mice lacking huntingtin in Wnt1 cell lineages.

Authors:  Paula Dietrich; Revathi Shanmugasundaram; E Shuyu; Ioannis Dragatsis
Journal:  Hum Mol Genet       Date:  2008-10-06       Impact factor: 6.150

7.  Congenital hydrocephalus and abnormal subcommissural organ development in Sox3 transgenic mice.

Authors:  Kristie Lee; Jacqueline Tan; Michael B Morris; Karine Rizzoti; James Hughes; Pike See Cheah; Fernando Felquer; Xuan Liu; Sandra Piltz; Robin Lovell-Badge; Paul Q Thomas
Journal:  PLoS One       Date:  2012-01-26       Impact factor: 3.240

Review 8.  Genetics of human hydrocephalus.

Authors:  Jun Zhang; Michael A Williams; Daniele Rigamonti
Journal:  J Neurol       Date:  2006-06-13       Impact factor: 4.849

Review 9.  The nexus of prematurity, birth defects, and intrauterine growth restriction: a role for plac1-regulated pathways.

Authors:  Michael E Fant; Juan Fuentes; Xiaoyuan Kong; Suzanne Jackman
Journal:  Front Pediatr       Date:  2014-02-21       Impact factor: 3.418

10.  Genetic and environmental factors in complex neurodevelopmental disorders.

Authors:  K M J van Loo; G J M Martens
Journal:  Curr Genomics       Date:  2007-11       Impact factor: 2.236

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